DeviceClearance

Product code EIG— Dental

BEACH GINGIVAL RETRACTION INSTR. TYPE B

Classification name
Retractor, All Types
Device class
Class 1
Regulation
21 CFR 872.4565
Advisory panel
Dental
Total cleared
8
First cleared
Most recent

Market context for product code EIG

FDA has cleared 8 devices under product code EIG between 1976 and 1997, filed by 7 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

Top applicants under product code EIG

Recent clearances under product code EIG

Data sourced from openFDA. This site is unofficial and independent of the FDA.